TY - JOUR
T1 - Cardiovascular Events Associated With SGLT-2 Inhibitors Versus Other Glucose-Lowering Drugs
T2 - The CVD-REAL 2 Study
AU - Kosiborod, Mikhail
AU - Lam, Carolyn S.P.
AU - Kohsaka, Shun
AU - Kim, Dae Jung
AU - Karasik, Avraham
AU - Shaw, Jonathan
AU - Tangri, Navdeep
AU - Goh, Su Yen
AU - Thuresson, Marcus
AU - Chen, Hungta
AU - Surmont, Filip
AU - Hammar, Niklas
AU - Fenici, Peter
AU - Cavender, Matthew A.
AU - Fu, Alex Z.
AU - Wilding, John P.
AU - Khunti, Kamlesh
AU - Norhammar, Anna
AU - Birkeland, Kåre
AU - Jørgensen, Marit Eika
AU - Holl, Reinhard W.
AU - Gulseth, Hanne Løvdal
AU - Carstensen, Bendix
AU - Bollow, Esther
AU - Franch-Nadal, Josep
AU - García Rodríguez, Luis Alberto
AU - Karasik, Avraham
AU - Tangri, Navdeep
AU - Kohsaka, Shun
AU - Kim, Dae Jung
AU - Arnold, Suzanne
AU - Goh, Su Yen
AU - Hammar, Niklas
AU - Fenici, Peter
AU - Bodegård, Johan
AU - Chen, Hungta
AU - Surmont, Filip
AU - Nahrebne, Kyle
AU - Blak, Betina T.
AU - Wittbrodt, Eric T.
AU - Saathoff, Matthias
AU - Noguchi, Yusuke
AU - Tan, Donna
AU - Williams, Maro
AU - Lee, Hye Won
AU - Greenbloom, Maya
AU - Kaidanovich-Beilin, Oksana
AU - Yeo, Khung Keong
AU - Chodick, Gabriel
AU - Melzer Cohen, Cheli
N1 - Publisher Copyright: © 2018 The Authors
PY - 2018/6/12
Y1 - 2018/6/12
N2 - Background: Randomized trials demonstrated a lower risk of cardiovascular (CV) events with sodium-glucose cotransporter-2 inhibitors (SGLT-2i) in patients with type 2 diabetes (T2D) at high CV risk. Prior real-world data suggested similar SGLT-2i effects in T2D patients with a broader risk profile, but these studies focused on heart failure and death and were limited to the United States and Europe. Objectives: The purpose of this study was to examine a broad range of CV outcomes in patients initiated on SGLT-2i versus other glucose-lowering drugs (oGLDs) across 6 countries in the Asia Pacific, the Middle East, and North American regions. Methods: New users of SGLT-2i and oGLDs were identified via claims, medical records, and national registries in South Korea, Japan, Singapore, Israel, Australia, and Canada. Propensity scores for SGLT-2i initiation were developed in each country, with 1:1 matching. Hazard ratios (HRs) for death, hospitalization for heart failure (HHF), death or HHF, MI, and stroke were assessed by country and pooled using weighted meta-analysis. Results: After propensity-matching, there were 235,064 episodes of treatment initiation in each group; ∼27% had established CV disease. Patient characteristics were well-balanced between groups. Dapagliflozin, empagliflozin, ipragliflozin, canagliflozin, tofogliflozin, and luseogliflozin accounted for 75%, 9%, 8%, 4%, 3%, and 1% of exposure time in the SGLT-2i group, respectively. Use of SGLT-2i versus oGLDs was associated with a lower risk of death (HR: 0.51; 95% confidence interval [CI]: 0.37 to 0.70; p < 0.001), HHF (HR: 0.64; 95% CI: 0.50 to 0.82; p = 0.001), death or HHF (HR: 0.60; 95% CI: 0.47 to 0.76; p < 0.001), MI (HR: 0.81; 95% CI: 0.74 to 0.88; p < 0.001), and stroke (HR: 0.68; 95% CI: 0.55 to 0.84; p < 0.001). Results were directionally consistent across both countries and patient subgroups, including those with and without CV disease. Conclusions: In this large, international study of patients with T2D from the Asia Pacific, the Middle East, and North America, initiation of SGLT-2i was associated with a lower risk of CV events across a broad range of outcomes and patient characteristics.
AB - Background: Randomized trials demonstrated a lower risk of cardiovascular (CV) events with sodium-glucose cotransporter-2 inhibitors (SGLT-2i) in patients with type 2 diabetes (T2D) at high CV risk. Prior real-world data suggested similar SGLT-2i effects in T2D patients with a broader risk profile, but these studies focused on heart failure and death and were limited to the United States and Europe. Objectives: The purpose of this study was to examine a broad range of CV outcomes in patients initiated on SGLT-2i versus other glucose-lowering drugs (oGLDs) across 6 countries in the Asia Pacific, the Middle East, and North American regions. Methods: New users of SGLT-2i and oGLDs were identified via claims, medical records, and national registries in South Korea, Japan, Singapore, Israel, Australia, and Canada. Propensity scores for SGLT-2i initiation were developed in each country, with 1:1 matching. Hazard ratios (HRs) for death, hospitalization for heart failure (HHF), death or HHF, MI, and stroke were assessed by country and pooled using weighted meta-analysis. Results: After propensity-matching, there were 235,064 episodes of treatment initiation in each group; ∼27% had established CV disease. Patient characteristics were well-balanced between groups. Dapagliflozin, empagliflozin, ipragliflozin, canagliflozin, tofogliflozin, and luseogliflozin accounted for 75%, 9%, 8%, 4%, 3%, and 1% of exposure time in the SGLT-2i group, respectively. Use of SGLT-2i versus oGLDs was associated with a lower risk of death (HR: 0.51; 95% confidence interval [CI]: 0.37 to 0.70; p < 0.001), HHF (HR: 0.64; 95% CI: 0.50 to 0.82; p = 0.001), death or HHF (HR: 0.60; 95% CI: 0.47 to 0.76; p < 0.001), MI (HR: 0.81; 95% CI: 0.74 to 0.88; p < 0.001), and stroke (HR: 0.68; 95% CI: 0.55 to 0.84; p < 0.001). Results were directionally consistent across both countries and patient subgroups, including those with and without CV disease. Conclusions: In this large, international study of patients with T2D from the Asia Pacific, the Middle East, and North America, initiation of SGLT-2i was associated with a lower risk of CV events across a broad range of outcomes and patient characteristics.
KW - SGLT-2 inhibitor
KW - death
KW - diabetes mellitus
KW - heart failure
KW - observational studies
KW - sodium glucose cotransporter-2 inhibitors
UR - http://www.scopus.com/inward/record.url?scp=85047499725&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.jacc.2018.03.009
DO - https://doi.org/10.1016/j.jacc.2018.03.009
M3 - مقالة
C2 - 29540325
SN - 0735-1097
VL - 71
SP - 2628
EP - 2639
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 23
ER -